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Atomfair 4-Ethyl-3-(trifluoromethyl)aniline C9H10F3N

Description 4-Ethyl-3-(trifluoromethyl)aniline (CAS No. 1389852-29-2) is a high-purity aromatic amine compound with the molecular formula C9H10F3N . This specialized chemical features an ethyl group and a trifluoromethyl group positioned ortho to the aniline moiety, offering unique reactivity and physicochemical properties. It is supplied as a clear to pale yellow liquid with a characteristic amine odor, and is rigorously tested to ensure ??95% purity (GC) for optimal performance in synthetic applications. Suitable for use as a versatile building block in pharmaceutical, agrochemical, and materials science research, this compound is packaged under inert gas to ensure stability and longevity. Store in a…

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Description

Description

4-Ethyl-3-(trifluoromethyl)aniline (CAS No. 1389852-29-2) is a high-purity aromatic amine compound with the molecular formula C9H10F3N. This specialized chemical features an ethyl group and a trifluoromethyl group positioned ortho to the aniline moiety, offering unique reactivity and physicochemical properties. It is supplied as a clear to pale yellow liquid with a characteristic amine odor, and is rigorously tested to ensure ??95% purity (GC) for optimal performance in synthetic applications. Suitable for use as a versatile building block in pharmaceutical, agrochemical, and materials science research, this compound is packaged under inert gas to ensure stability and longevity. Store in a cool, dry place away from light and oxidizing agents.

  • CAS No: 1389852-29-2
  • Molecular Formula: C9H10F3N
  • Molecular Weight: 189.18
  • Exact Mass: 189.07653381
  • Monoisotopic Mass: 189.07653381
  • IUPAC Name: 4-ethyl-3-(trifluoromethyl)aniline
  • SMILES: CCC1=C(C=C(C=C1)N)C(F)(F)F
  • Synonyms: 4-ethyl-3-(trifluoromethyl)aniline, 74422-98-3, SCHEMBL282158, 4-ethyl-3-trifluoromethyl-phenylamine, BS-45749

Application

4-Ethyl-3-(trifluoromethyl)aniline serves as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its electron-withdrawing trifluoromethyl group. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions and as a precursor for heterocyclic compounds. Researchers also utilize this compound in the development of liquid crystals and advanced polymer materials, where its structural motifs enhance thermal and chemical resistance.

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